Attenuation of Ni(0) Decomposition: Mechanistic Insights into AgF-Assisted Nickel-Mediated Silylation

被引:13
作者
Balakrishnan, Venkadesh [1 ]
Murugesan, Vetrivelan [1 ]
Chindan, Bincy [1 ]
Rasappan, Ramesh [1 ]
机构
[1] Indian Inst Sci Educ & Res Thiruvananthapuram, Sch Chem, Thiruvananthapuram 695551, Kerala, India
关键词
CROSS-COUPLING REACTIONS; OXIDATIVE ADDITION; GRIGNARD-REAGENTS; ALKYL-HALIDES; ARYL HALIDES; CRUCIAL ROLE; COMPLEXES; NI(I); ARYLATION; CATALYSIS;
D O I
10.1021/acs.inorgchem.1c03108
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In nickel-mediated Kumada cross-coupling reactions, low valent active nickel complexes are often generated in situ and the ligands usually govern the reactivity or stability of these complexes. However, the decomposition of active nickel complexes is inevitable if the subsequent reaction is sluggish. While we recently developed AgF-assisted nickel catalysis to cross-couple methyl ethers and silylmagnesium reagents, the intriguing catalytic role of AgF and the actual active nickel species remains elusive. Recently, both Ni(0) and Ni(I) intermediate complexes are identified as active species in Kumada cross-coupling reactions. Control experiments in combination with P-31 nuclear magnetic resonance (NMR) suggest that AgF attenuates the decomposition of in situ generated Ni(0) species. The plausible Ni(0) and Ni(I) intermediate complexes were synthesized, and experimental findings are consistent with the actual catalytic cycle being Ni(0)/Ni(II) rather than Ni(I)/Ni(III).
引用
收藏
页码:1438 / 1446
页数:9
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